Our mission is to regulate medicines, medical devices, and biological products throughout their lifecycle.
We are focusing on implementing changes.
These will make sure that there is:
- greater emphasis on transparency of regulatory decision-making processes
- continued focus on business process reform and a
- more strategic approach to the use of information technology to support regulatory operations.
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PageSponsor guidance materials relating to the regulatory framework for complementary medicines.
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PageThe medical devices reforms aim to enhance the safety, performance, and quality of medical devices in Australia and focus on patient safety.
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PageOverview and management of the EU European Union Medical Devices Regulation (MDR) transition under the Australian regulatory framework.
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PageWe will recognise the extended transition for the European Union In Vitro Diagnostic Medical Device Regulation (EU IVDR).
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PageInformation about reforms to the regulation of prescription medicines.
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PageWe're undertaking measures to improve how sunscreens are regulated in Australia so that consumers can be confident that sunscreens are effective and safe to use.
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